40 results · 30ms · Sources: EU EUDAMED, US FDA

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G-CATH TISSUE ANCHOR DELIVERY CATHETER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169413726·BLADE 5102916 29MM WIDE VESSELBLADE 16CM

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964076879·The ENDO CARRY-ON Procedure Kit contains all of...

Plateau Spacer System

FDA UDI
Life Spine, Inc.·00190837026936·PLATEAU Interbody, Curved, Bulleted, 11mm 29mm ...

SURGI-VISION PROSTATE COIL

FDA 510(k)
FDA Class 2 ·Radiology

FRONTIER ANTERIOR SCOLIOSIS SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

HLM TUBING SET

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015

VKMO 70000 #QUADROX-I HMO 70000+VHK71

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015

BO-HQV 70600#ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015

BO-HQV #70600ADULT PACK

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015

BO-HQV 70600#ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015

BO-HQV 70600#ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015

VKMO 11000

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015

BO-HQV 70600 ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 15, 2015

RESERVOIR VHK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 28, 2015

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 25, 2012

VENOUS HARDSHELL CARDIOTOMY RESERVOIR

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTM·September 13, 2016

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·May 9, 2013

BREZE2

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·September 19, 2014

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 4, 2011